Medical Device Recalls
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1 result found
510(K) Number: K003201 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BioTex Reusable Adapter Kit, Part Number 401-021-1010, packaged non-sterile in a dedicated case for ... | 2 | 03/24/2016 | Medtronic Navigation, Inc. |
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